Variant report

Variant	rs11188124
Chromosome Location	chr10:96760180-96760181
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 128 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:125)

rs_ID	r²[population]
rs10509681	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188148	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188153	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188154	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572064	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572080	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572082	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572094	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572107	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572116	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572128	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572150	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572168	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572169	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11572174	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11591385	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11592225	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11593816	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11596254	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11596290	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11596296	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11596943	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11598823	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11599203	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11599738	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12761315	1.00[ASN][1000 genomes]
rs12762602	1.00[ASN][1000 genomes]
rs12762652	1.00[ASN][1000 genomes]
rs12763201	1.00[ASN][1000 genomes]
rs12774244	1.00[ASN][1000 genomes]
rs12779339	1.00[ASN][1000 genomes]
rs12780333	1.00[ASN][1000 genomes]
rs17442862	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17443251	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17523627	1.00[ASN][1000 genomes]
rs17524348	1.00[ASN][1000 genomes]
rs1799853	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1934954	1.00[ASN][1000 genomes]
rs1934966	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2153629	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2185570	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2860968	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34246390	1.00[ASN][1000 genomes]
rs34254643	1.00[ASN][1000 genomes]
rs34320910	1.00[ASN][1000 genomes]
rs34462937	1.00[ASN][1000 genomes]
rs34949438	1.00[ASN][1000 genomes]
rs35238981	1.00[ASN][1000 genomes]
rs35461306	1.00[ASN][1000 genomes]
rs35883122	1.00[ASN][1000 genomes]
rs35955220	1.00[ASN][1000 genomes]
rs35998772	1.00[ASN][1000 genomes]
rs36037322	1.00[ASN][1000 genomes]
rs36042065	1.00[ASN][1000 genomes]
rs36168663	1.00[ASN][1000 genomes]
rs3980257	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs41291560	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4351748	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4433504	0.81[AFR][1000 genomes]
rs4607998	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4917636	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4918704	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4918705	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4918710	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4918716	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4918746	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4918795	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55727865	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55753924	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55777838	0.84[AMR][1000 genomes]
rs55804705	0.91[AMR][1000 genomes]
rs56028148	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56044736	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56090603	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56380192	1.00[ASN][1000 genomes]
rs56386142	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56408997	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs601746	1.00[ASN][1000 genomes]
rs61886257	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61886771	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61886773	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61886796	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61886797	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61886802	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61888362	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61888394	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61888396	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61888402	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61888408	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61888409	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61888410	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61888411	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs659309	1.00[ASN][1000 genomes]
rs66648066	1.00[ASN][1000 genomes]
rs670565	1.00[ASN][1000 genomes]
rs67728892	1.00[ASN][1000 genomes]
rs67851687	1.00[ASN][1000 genomes]
rs67918795	1.00[ASN][1000 genomes]
rs7082506	1.00[ASN][1000 genomes]
rs71482344	1.00[ASN][1000 genomes]
rs72816690	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72816698	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72816700	1.00[ASN][1000 genomes]
rs72816701	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72818612	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72818618	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72818642	0.86[AMR][1000 genomes]
rs72818651	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72818652	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72818673	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72818680	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72818681	1.00[ASN][1000 genomes]
rs72820645	1.00[ASN][1000 genomes]
rs73321646	0.93[AFR][1000 genomes]
rs73327336	0.81[AFR][1000 genomes]
rs9332100	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9332101	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9332102	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9332119	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9332155	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9332163	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9332179	1.00[ASN][1000 genomes]
rs9332216	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9332222	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9332242	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1035409	chr10:96495177-96832057	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96758400-96760800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:96759400-96760200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr10:96759400-96760200	Enhancers	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links